Change in FVC and survival in chronic fibrotic hypersensitivity pneumonitis

Thorax. 2018 Apr;73(4):391-392. doi: 10.1136/thoraxjnl-2017-210035. Epub 2017 Sep 7.

Abstract

The predictive value of the decline in FVC by ≥10% on survival in patients with fibrotic hypersensitivity pneumonitis is unknown. Of 112 patients included, 66 (59%) had surgical lung biopsies. Patients with ≥10% decline in predicted FVC after 6-12 months had a significantly increased risk of all-cause mortality (median survival 53 months, 95% CI 37 to 69 vs 139 months, 95% CI 66 to 212 months, p=0.007). On multivariate analysis remained associated with increasing mortality: decline in FVC by ≥10% (HR 4.13, 95% CI 1.96 to 8.70, p=0.005), lower FVC% (HR 1.03, 95% CI 1.01 to 1.05, p=0.003) and with decreasing mortality improvement with antigen avoidance (HR 0.18, 95% CI 0.04 to 0.77, p=0.021).

Keywords: hypersensitivity pneumonitis.

Publication types

  • Comparative Study
  • Letter

MeSH terms

  • Adult
  • Aged
  • Bronchoalveolar Lavage
  • Female
  • Follow-Up Studies
  • Humans
  • Idiopathic Pulmonary Fibrosis / diagnosis*
  • Idiopathic Pulmonary Fibrosis / mortality*
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Retrospective Studies
  • Tomography, X-Ray Computed* / methods
  • Vital Capacity*